Variant · Snv
LAMB2 NM_002292.4(LAMB2):c.712+88G>A
CI-VAR-00169622Explore in graph →NM_002292.4:c.712+88G>AClinVar 981940 rs138285969
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 981940 | drug response | no assertion criteria provided | 0 | Corticosteroids response; Lung cancer; Cervical cancer; Familial cancer of breast; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Acute myeloid leukemia | germline/somatic | 2 | Jan 12, 2020 | clinvar |